Package 70518-2132-0

Brand: losartan potassium

Generic: losartan potassium
NDC Package

Package Facts

Identity

Package NDC 70518-2132-0
Digits Only 7051821320
Product NDC 70518-2132
Product ID 70518-2132_49d94f9d-4d6a-325c-e063-6294a90a1a8d
Description

30 TABLET, FILM COATED in 1 BLISTER PACK (70518-2132-0)

Marketing

Marketing Status
Marketed Since 2019-06-05
Brand losartan potassium
Generic losartan potassium
Sample Package No

Linked Drug Pages (1)

Losartan Potassium ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "49d94f9d-4d6a-325c-e063-6294a90a1a8d", "openfda": {"unii": ["3ST302B24A"], "rxcui": ["979485"], "spl_set_id": ["f7cf8a7d-90f1-46a3-abff-1eb316aa7d72"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BLISTER PACK (70518-2132-0)", "package_ndc": "70518-2132-0", "marketing_start_date": "20190605"}], "brand_name": "Losartan Potassium", "product_id": "70518-2132_49d94f9d-4d6a-325c-e063-6294a90a1a8d", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Angiotensin 2 Receptor Antagonists [MoA]", "Angiotensin 2 Receptor Blocker [EPC]"], "product_ndc": "70518-2132", "generic_name": "Losartan Potassium", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Losartan Potassium", "active_ingredients": [{"name": "LOSARTAN POTASSIUM", "strength": "25 mg/1"}], "application_number": "ANDA090083", "marketing_category": "ANDA", "marketing_start_date": "20190605", "listing_expiration_date": "20271231"}